| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70592 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:130807780-130809940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr9:130809702-130809719 | TAGGTCACCACGACCTG | + | 7.04 | | ESR2 | MA0258.2 | chr9:130809703-130809718 | AGGTCACCACGACCT | + | 6.56 | | Nr2f6(var.2) | MA0728.1 | chr9:130809890-130809905 | TGAACTCCTGACCTC | - | 6.22 | | Nr5a2 | MA0505.1 | chr9:130807917-130807932 | GGGTTCAAGGCCAGC | + | 7.23 | | Sox3 | MA0514.1 | chr9:130809441-130809451 | AAAACAAAGG | - | 6.02 | | TBX20 | MA0689.1 | chr9:130808159-130808170 | CTTCACACCTA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 130808201 | 130808495 | | chr9 | 130809494 | 130809792 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I128045 | chr9 | 130808214 | 130810930 |
|
Enhancer Sequence | AAGCACTTAA AAAGAAGCTC TACCCCATTA GTCTTAGTGA CATGCAAACT AAAACCACAA 60
TGACACCAGG TGAGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGAC TAAGTTGGAT 120
GAATCATCTG AGGTCAGGGG TTCAAGGCCA GCCTGGCCAA CATGGCGAAA CCCCGTCTCT 180
ACTGAAAATA CAAAAATTAG CCAGGCATGG TGGTGCACGC CTGTAGTCCC AACTACTCGG 240
GAGGCTGAGG CATGAGACTT GCTTGAACCT GGGAGACAGA GGTTGCAGTG AGCTGAGGTG 300
GTGCTACTGC ACTCCAGCCC AGGTGACGAA GCAAGACCCT GTCTCCAAAA AAAAAAAAAA 360
AACCCACAAT GAGATACCAC TTCACACCTA CTAGAAATGG TTAAAGTTAG GAAGACTGAC 420
CAACTGACCA TACACCAAAT GTTGGCAAGG ATGTGGAACC ACTGGAACTC ACATACCCTG 480
TTGGTACTAA TGTAAAATGG TACAACCACA TTGGAAACAG TGTGGCAGTT AAACATACAC 540
TAACCATATG ATCCAGCTAT TTCACTCCTG GGCATTTAGC CAAGAGGAAT GAAGGCATGT 600
GTCCCCACAA AGACTTGTAC AACAAGGGTT CATAGCTACT AAATAATGGA AGCAACTAAA 660
ATATCCATCA ATATGCAATT GAAGCCTAGT GCAGTGGTTC ACGTCTGTAA TCCTGACACT 720
TTGGAGGCCA AGGCGGGCAG ATCACGTGAA GTCAGGAGTT TGATACCGGC CTGGCCAACA 780
TGGTGAAACC TCCGTCTCTA CTAAAAATAC AAAAAAATTA GCCAGACATG GTGGCATACA 840
CCTGTAATCC CAGCTAATCG GGAGGCTGAA GCAGGAGAAT CGCTTGAACC TGGGAGGCAG 900
AGGTTGCAAG ACCATATCAC TGCCCTCCAG TCTAAGTAAC AGAGTGAGAC TCTGTCTCAA 960
AAAAAAAAAA AGCGATTGAA TAGATAAACA AATTATGGTA TAACAATTCT GTGATAAAGG 1020
AGCAAACTTT TTTTTTTTCT GAGAGGTCTT GCTCTGTTGC CGAGGCTGTG AATGAGCTAT 1080
TAAGACCCAC AACATGGATG CATCTCACAA TAATTAGGCT GAGTGAAAAA AGCCAGACAG 1140
AGAAAGAGCA CAGGCTGCAT GATTTCATTT ATGTAAAATT CTGGAAAATG CAATTAATCT 1200
ACAGTGACAG AAAGCAGACC AGTGACTGCT TGGAGTGGAG GCGGGAGGGC GTGGAGAGGG 1260
AATGGGAATG GGGAAGGAGG GATGATTATA TACAGGGGTC ACCAGGAAAC TTGGCAGTGA 1320
TGGAGCTTTT TATGACAATT CTCATGGTCT TTTTTTTTTT TTTTTTTTTT TGAGACAGAG 1380
TCTTGCTCTG TTGCCCAGGC TGGGGTGCAG TGGCATGATC TTGGCTCACT GCAGCCTCTG 1440
CCTCCCGGGT TCAAGTGATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA TTACAGGCGT 1500
CCACCACCAC TGTTGCAGGA AACAGAGGAC CAGAGAGACC AATATGGGTG AATACAGGAG 1560
GATGGTTATT AAGGTGCACA CCGGCTCAGT GGATTCACAT CCAAAAAGCT GAGCATTGAA 1620
CAAAAACAGA TTTTAGCTTA TATAGGCTAG CATACAAAAG CAAAACAAAG GCAGTGAATT 1680
TTACAGTGAC AAGTCACATA ATCCATAGTA TAGCTGCTGA CCTGGCACTA ACCTATGGCC 1740
TTGCATAGCT AGTGGCCTAG CAGTGGCATC GAAAGAAAAG CAGGAACTTT GCAAATCTTA 1800
CTAAATACAA CCATTGGCAA ACATGGCCAT AACTAATAGT TCAGTACATG AGAGACAGTA 1860
AAGGAATTTG TTTTTCTTCT TTTAACTTTG CTCGGGGGTG TCTGGAGCTG ATTTCTGCAG 1920
GCTAGGTCAC CACGACCTGT CTATAGCCTT GCTTGCAGCA GTGAAAAACG TGTTTTTCGC 1980
TTAACCCTTA CTTTCCTTGG AGTGAATAAA CGCAGTATTT ATTTTTCTTT AAATTTCTGC 2040
CTCAACACAC TTGGCTAATT TTTGTATTTT TAGTAGAGAC AGGGTCTCAC CATGTTGGCC 2100
AGGCTGATCT TGAACTCCTG ACCTCAGGTG ATCCACCCGC CTCAGCTTCA CAAAGTTCTG 2160
|
